TACC3
transforming acidic coiled-coil containing protein 3
Summary
This gene encodes a member of the transforming acidic colied-coil protein family. The encoded protein is a motor spindle protein that may play a role in stabilization of the mitotic spindle. This protein may also play a role in growth a differentiation of certain cancer cells. [provided by RefSeq, Nov 2011]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35624862 | 4:1,725,160 | G/A | — | benign |
| rs781449365 | 4:1,725,222 | C/T | — | uncertain significance |
| rs905523646 | 4:1,725,246 | C/A | — | uncertain significance |
| rs373800152 | 4:1,725,257 | C/G | — | uncertain significance |
| rs756373513 | 4:1,725,305 | A/G | — | uncertain significance |
| rs759970838 | 4:1,725,476 | C/T | — | uncertain significance |
| rs1273470515 | 4:1,725,514 | G/A | — | uncertain significance |
| rs933226916 | 4:1,725,525 | T/C | — | uncertain significance |
| rs577000546 | 4:1,725,551 | A/G | — | uncertain significance |
| rs2546713322 | 4:1,729,442 | C/G | — | uncertain significance |
| rs1172300113 | 4:1,729,496 | G/A | — | uncertain significance |
| rs531939381 | 4:1,729,595 | A/G | — | uncertain significance |
| rs1312130512 | 4:1,729,610 | C/G | — | uncertain significance |
| rs764747004 | 4:1,729,638 | C/T | — | uncertain significance |
| rs376412171 | 4:1,729,647 | A/G | — | uncertain significance |
| rs767170101 | 4:1,729,690 | T/A | — | uncertain significance |
| rs757798309 | 4:1,729,697 | T/G | — | uncertain significance |
| rs770678022 | 4:1,729,740 | A/T | — | uncertain significance |
| rs1717783436 | 4:1,729,772 | G/A | — | uncertain significance |
| rs766758472 | 4:1,729,783 | C/G | — | uncertain significance |
| rs781180810 | 4:1,729,790 | G/A | — | likely benign |
| rs2546714430 | 4:1,729,796 | G/C | — | uncertain significance |
| rs752880541 | 4:1,729,799 | T/C | — | uncertain significance |
| rs770804478 | 4:1,729,815 | C/T | — | uncertain significance |
| rs759748375 | 4:1,729,839 | G/C | — | uncertain significance |
| rs1011823920 | 4:1,729,868 | G/C | — | uncertain significance |
| rs200427394 | 4:1,729,875 | C/T | — | uncertain significance |
| rs369399901 | 4:1,729,880 | C/A | — | uncertain significance |
| rs139849008 | 4:1,729,887 | G/T | — | uncertain significance |
| rs775733820 | 4:1,729,910 | G/A | — | uncertain significance |
| rs144462438 | 4:1,729,911 | G/A | — | benign |
| rs145840927 | 4:1,729,979 | C/T | — | uncertain significance |
| rs199937898 | 4:1,729,986 | A/G | — | uncertain significance |
| rs772523787 | 4:1,730,007 | G/T | — | uncertain significance |
| rs1302773987 | 4:1,730,118 | C/T | — | uncertain significance |
| rs200203771 | 4:1,730,121 | C/G | — | uncertain significance |
| rs777262465 | 4:1,730,129 | G/A | — | uncertain significance |
| rs1287418584 | 4:1,730,183 | C/T | — | uncertain significance |
| rs116204682 | 4:1,730,262 | C/T | — | benign |
| rs377096121 | 4:1,730,270 | G/A | — | uncertain significance |
| rs755526449 | 4:1,730,282 | G/A | — | uncertain significance |
| rs1448914867 | 4:1,730,309 | C/A | — | uncertain significance |
| rs780833702 | 4:1,730,360 | G/A | — | uncertain significance |
| rs199671695 | 4:1,730,420 | C/G | — | uncertain significance |
| rs770763829 | 4:1,730,475 | C/T | — | uncertain significance |
| rs1418842095 | 4:1,730,477 | G/C | — | uncertain significance |
| rs116328109 | 4:1,732,604 | G/C | — | benign |
| rs1217481602 | 4:1,732,639 | G/A | — | uncertain significance |
| rs779615051 | 4:1,732,655 | A/C | — | uncertain significance |
| rs541201025 | 4:1,732,670 | C/T | — | uncertain significance |
| rs565679658 | 4:1,732,685 | G/C | — | uncertain significance |
| rs776833740 | 4:1,732,923 | A/T | — | uncertain significance |
| rs899250002 | 4:1,732,965 | A/C | — | likely benign |
| rs798766 | 4:1,734,239 | T/C | intron variant | — |
| rs28499138 | 4:1,736,737 | T/C | upstream gene variant | — |
| rs116852708 | 4:1,737,009 | C/T | — | uncertain significance |
| rs34612262 | 4:1,737,013 | C/T | — | benign |
| rs757267468 | 4:1,737,014 | G/A | — | uncertain significance |
| rs144932072 | 4:1,737,481 | G/C | — | uncertain significance |
| rs141231740 | 4:1,737,542 | G/A | — | uncertain significance |
| rs371729680 | 4:1,738,975 | G/A | — | uncertain significance |
| rs1718318964 | 4:1,738,988 | C/T | — | uncertain significance |
| rs151225636 | 4:1,738,999 | C/T | — | likely benign |
| rs140344901 | 4:1,739,004 | G/A | — | likely benign |
| rs144084158 | 4:1,739,005 | C/T | — | uncertain significance |
| rs62285111 | 4:1,739,028 | C/T | — | benign |
| rs114631890 | 4:1,739,053 | C/G | — | uncertain significance |
| rs1403373016 | 4:1,739,328 | C/G | — | uncertain significance |
| rs1473905990 | 4:1,739,335 | C/A | — | uncertain significance |
| rs754513840 | 4:1,739,352 | G/A | — | uncertain significance |
| rs770552553 | 4:1,739,365 | C/T | — | uncertain significance |
| rs945665087 | 4:1,739,425 | C/A | — | uncertain significance |
| rs2546735380 | 4:1,741,469 | G/A | — | uncertain significance |
| rs1332950951 | 4:1,741,483 | C/T | — | uncertain significance |
| rs901814528 | 4:1,742,585 | G/A | — | uncertain significance |
| rs1419297079 | 4:1,742,672 | C/T | — | uncertain significance |
| rs11736125 | 4:1,744,939 | C/T | downstream gene variant | — |
| rs12511923 | 4:1,745,152 | C/T | downstream gene variant | — |
| rs1169162345 | 4:1,746,281 | C/G | — | uncertain significance |
| rs777517232 | 4:1,746,331 | C/G | — | uncertain significance |
| rs144776052 | 4:1,746,456 | C/A | — | benign |
| rs371593137 | 4:1,746,480 | C/T | — | uncertain significance |
| rs765035882 | 4:1,746,503 | A/G | — | uncertain significance |
| rs560532692 | 4:1,746,567 | C/T | — | benign |
| rs1425327015 | 4:1,746,733 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.